Canonical Allele Identifier: CA382436238

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922239A>G (hg19) ; chr11:g.101051508A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051508A>G , CM000673.2:g.101051508A>G	GRCh38
NC_000011.9:g.100922239A>G , CM000673.1:g.100922239A>G	GRCh37
NC_000011.8:g.100427449A>G	NCBI36
NG_016475.1:g.83306T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2273T>C MANE Select	ENSP00000325120.5:p.Leu758Ser
ENST00000263463.9:c.1967T>C	ENSP00000263463.5:p.Leu656Ser
ENST00000325455.9:c.2273T>C	ENSP00000325120.5:p.Leu758Ser
ENST00000526300.5:c.1967T>C	ENSP00000436803.1:p.Leu656Ser
ENST00000528960.5:c.2156T>C	ENSP00000432914.1:p.Leu719Ser
ENST00000533207.5:n.1640T>C
ENST00000534013.5:c.491T>C	ENSP00000436561.1:p.Leu164Ser
ENST00000534780.5:c.2273T>C	ENSP00000432352.1:p.Leu758Ser
ENST00000617858.4:c.1967T>C	ENSP00000481227.1:p.Leu656Ser
ENST00000619228.2:c.2156T>C	ENSP00000482698.1:p.Leu719Ser
NM_000926.4:c.2273T>C MANE Select	NP_000917.3:p.Leu758Ser
NM_001202474.3:c.1781T>C	NP_001189403.1:p.Leu594Ser
NM_001271161.2:c.1475T>C	NP_001258090.1:p.Leu492Ser
NM_001271162.1:c.491T>C	NP_001258091.1:p.Leu164Ser
NR_073141.2:n.2266T>C
NR_073142.2:n.2149T>C
NR_073143.2:n.1960T>C
XM_006718858.2:c.2273T>C	XP_006718921.1:p.Leu758Ser
XR_947831.1:n.3954T>C
XM_006718858.3:c.2273T>C	XP_006718921.1:p.Leu758Ser
NM_001271162.2:c.491T>C	NP_001258091.1:p.Leu164Ser
NR_073141.3:n.2280T>C
NR_073142.3:n.2163T>C
NR_073143.3:n.1974T>C